Senior Manager role focused on designing, developing, and deploying AI agents for enterprise workflow automation, decision enhancement, and intelligent user interactions. Requires experience with agentic orchestration frameworks, vector databases, RAG, and LLM principles, along with leadership in managing technical teams and delivering enterprise-scale projects.

AI/ML Engineer role focused on vaccine research, applying AI/ML to discover and develop vaccines. Responsibilities include shaping scientific strategy with AI, owning foundational and predictive modeling end-to-end, advancing generative AI for vaccine design, engineering robust ML systems, decoding high-dimensional biology, and elevating AI fluency. Requires PhD or Master's with experience in AI/ML within life sciences, knowledge of vaccine R&D, and expertise in foundation models, generative AI, and ML system design.

This role focuses on building and deploying production-grade full-stack applications that integrate LLM and AI capabilities into pharmaceutical research workflows. Responsibilities include developing backend services for data processing, embedding generation, vector search, and LLM orchestration, creating frontend interfaces, implementing RAG systems and agentic LLM architectures, and deploying/maintaining systems on AWS. The role also involves contributing to semantic frameworks and conceptual research.

Senior Manager, Applied AI Workflow Scientist at Pfizer, focused on applying LLMs and agentic AI to scientific use cases in Inflammation & Immunology. The role involves identifying high-value scientific applications, building reusable AI workflows and agentic systems, and partnering with scientists to ensure adoption and impact. It emphasizes practical application, scientific credibility, user partnership, and scalable workflows.

Director of AI Engineering role focused on applying AI automation and advanced analytics in regulated healthcare R&D operations. The role involves leading the definition and delivery of AI solutions for lab and office workflows, strengthening operational decision-making through predictive models, enabling regulated AI systems with governance, optimizing development planning, and engineering/scaling production-grade ML platforms. Requires expertise in predictive modeling, optimization, automation, generative AI, and ML system design, with strong programming skills in Python and ML frameworks, and experience scaling models in cloud/HPC environments. Collaboration across scientific, operational, quality, and business teams is critical.

Internship role supporting data analytics, business intelligence, and AI-enabled initiatives within Pfizer's Commercial Excellence & Innovation team. Focuses on improving data quality, translating data into insights, and supporting early AI/advanced analytics use cases in a regulated environment. Involves data preparation, analysis using Python/SQL, and exposure to ML concepts, LLMs, and AI agents.

AI Data Engineer focused on Computational Toxicology at Pfizer. The role involves applying Data Engineering and MLOps best practices to automate scientific workflows, curate AI-ready datasets, and enable scalable AI solutions for drug safety science. This includes preparing, structuring, and validating data for AI-enabled toxicology assessments, integrating multi-modal datasets, and implementing scalable data pipelines.

This role is for a Senior Manager, AI and Data Science Solution Engineer at Pfizer in Greece. The primary focus is on implementing technology solutions across various functions, coordinating with delivery engineers, acting as a technical interface, developing user stories, and assisting with test execution. While the role involves using AI tools and understanding responsible AI practices, it does not involve core AI/ML model development or research.

This is a 15-month training program for mid-career professionals in biopharmaceutical manufacturing. The trainee will support the development, implementation, and improvement of industrial automation and digital solutions, including AI-enabled systems, under supervision. The role focuses on building a foundation in automation, digital technologies, and the responsible use of Generative AI within regulated frameworks.

This role is for a senior software engineer who will design, build, and maintain software systems, leveraging AI tools to enhance productivity and verifying AI-generated code. The role involves being embedded with business units (Commercial, Manufacturing, R&D) to act as a 'startup CTO', bridging product building and business problem-solving. Responsibilities include driving technical initiatives, developing technical leaders, shaping technology-driven business strategy, designing AI-augmented engineering workflows, establishing reliability and documentation standards, and driving process efficiency. The role emphasizes curiosity, outcome ownership, polymath orientation, precision communication, and systems thinking, with expert-level skills in business immersion, data integration, full-stack development, multi-audience communication, problem discovery, rapid prototyping, stakeholder management, and team collaboration. Practitioner-level skills include AI evaluation and verification.

This role focuses on designing, prototyping, and developing laboratory automation solutions for process development in healthcare, leveraging technologies like computer vision and machine learning. It involves integrating automated hardware, implementing robotic control and data management systems, and using coding languages like Python or C++ for AI/ML applications. The goal is to enhance automation for laboratory experimentation and drug development workflows.

This role focuses on implementing and overseeing the GCP Quality Management System (QMS) for clinical development activities in China. It involves ensuring compliance with global standards and regulatory requirements, managing inspections and audits, and providing vendor quality oversight. A key aspect is contributing to digital and AI initiatives, supporting AI-enabled processes like Site Start-Up, participant recruitment, eSource, and data analysis, with the goal of improving quality and operational efficiency in clinical development.

The Associate MQA Downstream role at Pfizer is responsible for ensuring quality and compliance with cGMP standards in pharmaceutical manufacturing processes, specifically in Terminal Sterilization, Visual Inspection, and Packing areas. This involves reviewing batch records, performing inspections, monitoring processes, and identifying areas for improvement to ensure product safety and patient care.

This role is responsible for executing content management of non-complex local product documents, local label documents, and patient leaflets for nationally registered products. It involves system management for labeling activities, QC of labeling text, and ensuring data integrity. The role requires basic knowledge of labeling and regulatory principles, proficiency in systems, and experience with structured data. Experience in Regulatory Affairs, particularly with product labeling and regulatory guidelines, is important.

Associate role in pharmaceutical manufacturing at Pfizer, focusing on supporting production processes, problem-solving, and ensuring quality and adherence to standards. Requires a High School Diploma/GED and 2+ years of experience, with bonus points for cGMP experience and familiarity with AI tools.

This role supports the Quality Organization by ensuring compliance with regulatory requirements, company quality systems, and cGMP. It focuses on continuous improvement, project leadership, and cross-functional partnerships to enhance compliance, efficiency, and inspection readiness in a pharmaceutical manufacturing environment.

Pfizer is seeking a Senior Director of Clinical Development Scientist to provide scientific oversight and ensure the quality of clinical trials in Internal Medicine. The role involves leading clinical execution, protocol development, data and safety review, and collaboration with various stakeholders including Health Authorities and KOLs. The position also requires managing clinical deliverables, ensuring TMF compliance, and potentially contributing to regulatory filings and publications. The role may also involve managing and mentoring other clinical colleagues.

Instrument Engineer role at Pfizer's biopharmaceutical manufacturing site in Strängnäs, Sweden. Responsibilities include developing, managing, and future-proofing plant instrumentation, ensuring compliance with quality standards and validated status. The role involves technical expertise, leading technical tasks, participating in qualification and deviation management, preventive maintenance planning, continuous improvement initiatives, and managing service agreements. Requires a technical degree or equivalent experience, expertise in instrumentation/metrology/electrical fields, understanding of measurement techniques and uncertainties, and experience in regulated environments (GMP is a plus). Strong communication skills in Swedish and English are necessary. The ideal candidate is structured, analytical, solution-oriented, responsible, and collaborative.

Lead people, technology, and financial resources in pharmaceutical manufacturing to achieve desired outcomes, ensuring adherence to SOPs, GMPs, and plant protocols. Manage investigations, corrective actions, and team performance while fostering continuous improvement and compliance.

Pfizer is seeking an Engineering Maintenance Technician in Dublin, Ireland, to manage maintenance and reliability engineering activities for utilities, buildings, and equipment. The role involves providing engineering support for project execution, operational support, reviewing work orders, conducting Root Cause Failure Analysis (RCFA), ensuring calibration compliance with Good Manufacturing Practices (GxP), and assisting in the development of the Preventative Maintenance program. The ideal candidate will have a Diploma/Degree in an Engineering/Technical Discipline or Electrical/Mechanical Trade Qualification, 3+ years of experience, and strong troubleshooting skills in mechanical and electrical systems, with desirable experience in commissioning, qualification, start-up, and process automation systems.

This role is for a Group Manager focused on Inspection Readiness within Pfizer's pharmaceutical operations in India. The primary responsibilities include managing the Site Quality Review program, overseeing CAPA management, ensuring compliance with regulations and GMP, and coordinating with global teams for inspection preparation. The role requires strong knowledge of pharmaceutical manufacturing, quality systems, and people management, with a minimum of 10 years of experience in the industry.

This role manages the process of creating and updating labeling artwork for pharmaceutical packaging, ensuring compliance with regulatory requirements and coordinating with various internal and external stakeholders. It involves initiating artwork requests, tracking changes, managing timelines, and ensuring accurate final content for product packaging.

Senior Manager, MAPP Technical Lead at Pfizer, responsible for the end-to-end architecture strategy of the MAPP compliance platform, ensuring alignment with business objectives and adherence to privacy and data protection requirements. This role involves guiding development teams, ensuring compliance with security and data governance frameworks, and identifying platform improvement opportunities.

This role is for a Senior Production Operator at Pfizer, responsible for operating, maintaining, and troubleshooting pharmaceutical manufacturing equipment. The position requires experience with cGMP, SOPs, and safety protocols, with a focus on ensuring production quality and efficiency. It involves hands-on mechanical work, data interpretation from control systems, and training new hires. The role is critical for delivering medicines to patients.

Supervisor responsible for leading downstream production of mAb products, ensuring targets, quality, compliance, cost standards, and customer service are met. This includes managing staff, planning, performance assessment, and employee counseling. Ensures work is accurate, timely, efficient, and compliant with corporate policies, SOPs, cGMP, and FDA regulations. Participates in investigations and continuous improvement initiatives using LEAN and Six Sigma. Optimizes resources for maximum production and ensures quality and safety standards.

Supervisor for downstream operations of mAb products in pharmaceutical manufacturing, focusing on production targets, quality, compliance, and team management. Ensures adherence to cGMP and FDA regulations, optimizes resources, and leads production staff.

This role is for an Assistant Associate in Engineering Stores at Pfizer, responsible for managing material receipts, storage, and issuance within the manufacturing logistics and supply team. The position involves using systems like SAP MM/EAMS/ARIBA, adhering to cGMP and safety procedures, and ensuring efficient material flow to support patient access to medicines. Key duties include inventory management, documentation, and supporting audits.

This role is for an Associate, Talent Acquisition at Pfizer in the Philippines, responsible for full-cycle recruitment from entry-level to Manager roles. The position involves managing end-to-end recruitment, stakeholder management, and ensuring a positive candidate experience. Key responsibilities include sourcing, selection, offer development, process compliance, and utilizing AI tools to enhance efficiency. The role requires strong organizational, communication, and problem-solving skills, with a preference for experience in the pharmaceutical industry and ATS platforms.

This role provides regulatory support for pharmaceutical products throughout their lifecycle, from initial registration to withdrawal. It involves managing regulatory dossiers, responding to health authority queries, and coordinating cross-functional activities for tenders, reporting, and launch planning. The position requires strong organizational skills, technical aptitude, and proficiency in Korean and English.

Senior QC Laboratory Analyst at Pfizer responsible for performing and reviewing analytical testing of raw materials, API samples, and in-process samples. The role involves adhering to cGMPs, ALCOA principles, and Data Integrity requirements, troubleshooting laboratory issues, and contributing to continuous improvement activities within a regulated healthcare environment.

This role focuses on managing the operational and regulatory aspects of clinical trial site activation and conduct at Pfizer. It involves coordinating essential documents, ensuring compliance with Good Clinical Practices (GCP) and local regulations, and managing communication between Pfizer, ethics committees, and investigator sites. The role requires a strong understanding of regulatory processes and documentation throughout the study lifecycle.

This role is responsible for ensuring the completeness, quality, and integrity of clinical trial data under a Risk-Based Monitoring (RBM) model. Key activities include developing and implementing RBM systems, defining and monitoring Key Risk Indicators (KRIs), processing and reviewing study data for signal and action management, and ensuring compliance with regulations and SOPs. The role requires technical expertise in clinical trial databases, data management processes, and system setup, as well as strong communication and project management skills.

Administrative Lead role at Pfizer supporting Vaccine R&D, responsible for day-to-day administrative and business support, calendar management, travel arrangements, meeting organization, procurement, document formatting, training on administrative procedures, and managing onboarding/offboarding logistics. Requires strong organizational, communication, and computer skills, with a minimum of 6 years of administrative experience.

Senior Manager, Data Protection Engineering role at Pfizer, focusing on leading and evolving data protection capabilities. Responsibilities include defining strategy, architecture, and control frameworks for DLP, data discovery, classification, and encryption. The role involves overseeing implementation of data protection technologies, ensuring security-by-design, supporting incident response, and collaborating with Privacy, Legal, and Compliance teams to meet regulatory requirements like GDPR, HIPAA, SOX, and GxP. Requires strong experience in cybersecurity, data protection controls, DLP, data classification, encryption, and cloud integration within regulated environments.

This role leads enterprise offensive security capabilities, including penetration testing, red teaming, and adversary simulation, to identify and prioritize security weaknesses in a highly regulated pharmaceutical environment. It involves partnering with detection and remediation teams to reduce risk and improve defensive outcomes.

Senior Utilities Technician role at Pfizer in Itapevi, SP, Brazil. Responsibilities include diagnosing and repairing equipment issues, performing scheduled preventive electrical maintenance, managing corrective maintenance backlog, identifying and implementing equipment improvements, verifying work results, managing spare parts procurement, and performing low and medium voltage electrical maintenance. The role also involves applying RFT concepts, teamwork, and adhering to Pfizer's manufacturing vision, mission, values, and safety standards. Requires a Technical degree in Electrical Engineering or equivalent, intermediate Excel, Word, PowerPoint, and technical English, with 5 years of prior experience, preferably in the pharmaceutical industry.

This role at Pfizer focuses on pharmaceutical manufacturing operations, ensuring compliance with cGMP, managing production schedules, supervising operators, and coordinating with other departments for efficient and quality-driven production of medicines. It requires a B Pharmacy degree and experience in manufacturing processes, particularly tablet manufacturing and packaging.

This role is responsible for performing method transfers, validations, and verifications of complex analytical techniques within a quality control setting at Pfizer. The Associate will interpret and evaluate data for accuracy, ensure compliance with cGMP and GLP, review and revise SOPs, and conduct analyses on finished products, raw materials, and components. The role requires a Bachelor's or Master's degree in Chemistry or Microbiology with relevant experience in analytical testing and a strong understanding of various analytical techniques and regulatory standards.

Associate Manager for Quality Control at Pfizer in India, focusing on ensuring product quality and compliance with GMP in laboratories. Responsibilities include test method validation, media preparation, sample testing, data review, and participation in cross-functional teams. Requires a Master's degree in Chemistry/Microbiology with 5-7 years of analytical testing experience, strong technical skills in method validation, and knowledge of pharmaceutical quality systems. Familiarity with AI tools is a plus.

Internship role focused on supporting and developing features for a web project, involving data cleansing, implementing visualizations, and automating processes. Requires current enrollment in a computer science or related bachelor's degree program and coding experience in JavaScript, Python, or TypeScript.

Senior Process Engineer role at Pfizer focused on leading product manufacturing campaigns, developing and modifying process formulations, methods, and controls to meet quality standards. Responsibilities include technical supervision, process improvements, troubleshooting, ensuring safety and GMP compliance, and collaborating with cross-functional teams in a pharmaceutical manufacturing environment.

This role is for a Senior Process Technician at Pfizer's manufacturing site expansion in Singapore. The technician will operate chemical/fermentation process equipment, perform quality control, handle hazardous materials, and ensure adherence to GMP/GDP standards. Responsibilities include monitoring processes, troubleshooting deviations, documentation, and participating in investigations and commissioning activities. The role requires a technical diploma or GCE 'O/A' levels, 3-5 years of relevant industry experience, and the ability to act decisively and independently.

Senior Associate Quality Assurance role at Pfizer focused on ensuring the quality and compliance of clinical and commercial drug batches. Responsibilities include reviewing batches, conducting statistical process control, approving investigations and change controls, managing projects, and ensuring adherence to GxP and cGMP standards.

This role at Pfizer focuses on Quality Systems, specifically document management and control within a regulated healthcare environment. While the role mentions using AI tools like ChatGPT for productivity, the core responsibilities do not involve building or directly deploying AI/ML models. The primary focus is on ensuring compliance with GMP, GLP, and GCP standards, managing documentation lifecycles, and supporting quality assurance functions.

This is a 15-month training program for Analytical Chemists in biopharmaceutical manufacturing. The role involves performing chemical analysis using various instruments, compiling and analyzing data, providing manufacturing support, working with vendors, and adhering to good laboratory practices and safety procedures. It is designed for fresh graduates or mid-career individuals with no prior experience in the biopharmaceutical sector.

Manager for Quality Assurance Batch Release in a pharmaceutical manufacturing facility, ensuring compliance with cGMP and overseeing daily release activities, exception reports, and team performance. Requires extensive experience in pharmaceutical quality systems and people management.

This is a 15-month training program for fresh or mid-career individuals to enter the biopharmaceutical manufacturing sector at Pfizer in Singapore. The role involves laboratory-scale experiments, process development, troubleshooting, and collaboration with various functions to ensure product quality and continuous improvement.

This is a QA Specialist role focused on compliance within pharmaceutical manufacturing. The role ensures adherence to Good Manufacturing Practices (GMP), Pfizer Quality Standards, and regulatory guidelines. Responsibilities include quality oversight of vendor management, managing inspections, collaborating with cross-functional teams, and maintaining quality systems. The position is part of a training program for advanced biopharmaceutical manufacturing professionals.